ClearanceBrief
510(k) K982826 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

MEGA 2000

ApplicantMegadyne Medical Products, Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, Nov 6, 1998
ReceivedAug 11, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982826

DateFirm and productCodeLinked 510(k)
Jun 30, 2023Megadyne Medical Products, Inc.
MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery
Open, Classified
GEINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.